Elalaoui Siham Chafai - Res Ctr Genom Human Pathol GENOPATH, Mohammed V Univ Rabat

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论文共 76 篇作者统计合作学者相似作者

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Identification of Novel and De Novo Variant in the SCN1A Gene Confirms Dravet Syndrome in Moroccan Child: a Case Report

Hinde El Mouhi,Nada Amllal,Meriame Abbassi,Ayoub Nedbour,Meryem Jalte,Jaber Lyahyai,Siham Chafai Elalaoui,Laila Bouguenouch,Sana Chaouki

Molecular Biology Reportsno. 1 (2024): 1-6

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First Nonsense Variant of MED12 Gene in a Female with Complete Maat-Kievit-Brunner Phenotype of Ohdo Syndrome: A Case Report

N. Amllal,J. Lyahyai,S. C. Elalaoui,A. Sefiani,I. Ratbi

GENE REPORTS (2024)

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Novel Splice Site Pathogenic Variant in STXBP1 Gene in a Child with Intellectual Disability, Epilepsy, and Autism Spectrum Disorder: A Case Report

Nada Amllal,Jaber Lyahyai,Siham Chafai Elalaoui,Youssef El Kadiri,Abdelaziz Sefiani

MOLECULAR SYNDROMOLOGY（2024）

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Novel Variant Related to SATB2-associated Syndrome

Nada Benyahya,Nada Amllal,Siham Chafai Elalaoui,Mustapha El Alloussi,Abdelaziz Sefiani,Jaber Lyahyai

International journal of developmental neuroscience the official journal of the International Society for Developmental Neuroscience (2024)

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A Series of Four Patients with Sotos Syndrome Harboring Novel NSD1 Mutations: Clinical and Molecular Description

Nada Amllal,Maria Zerkaoui,Wafaa Jdioui,Siham Chafai Elalaoui,Abdelaziz Sefiani,Jaber Lyahyai

Molecular Biology Reportsno. 1 (2024): 1-7

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Misdiagnosis of tracher-collins syndrome initially attributed to drug teratogenicity: a moroccan case report

A. Lamzouri,A. E. L. Rherbi,I Ratbi,F. Z. Laarabi, R. Chahboune,S. C. Elalaoui, H. Hamdaoui, R. S. Bencheikh,A. Sefiani

BALKAN JOURNAL OF MEDICAL GENETICS（2023）

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Early Diagnosis of Congenital Muscular Pathologies Using Next-Generation Sequencing: Experiences from a Tertiary Center in Morocco

Youssef El Kadiri,Ilham Ratbi,Mouna Ouhenach,Siham Chafai Elalaoui,Imane Cherkaoui Jaouad,Abdelali Zrhidri,Maryem Sahli,Nazha Birouk,Abdelaziz Sefiani,Jaber Lyahyai

The Egyptian Journal of Medical Human Genetics /The Egyptian Journal of Medical Human Genetics（2023）

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Identification of Novel and De Novo Mutation in the SCN1A Gene By Exome Sequencing Confirms Dravet Syndrome in Moroccan Child: A Case Report

Hinde El Mouhi,Nada Amllal,Meriame Abbassi,Ayoub Nedbour,Meryem Jalte,Jaber Lyahyai,Siham Chafai Elalaoui,Laila Bouguenouch,S. Chaouki

Research Square (Research Square) (2023)

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Identification of Two Novel ANKRD11 Mutations: Highlighting Incomplete Penetrance in KBG Syndrome

Nada Amllal,Siham Chafai Elalaoui,Maria Zerkaoui,Amal Chiguer,Lamia Afif, Amal Thimou Izgua,Abdelaziz Sefiani,Jaber Lyahyai

Annals of laboratory medicine（2023）

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Mutational Spectrum of BRCA1/2 Genes in Moroccan Patients with Hereditary Breast And/or Ovarian Cancer, and Review of BRCA Mutations in the MENA Region

Siham Chafai Elalaoui, Fatima Zohra Laarabi, Lamiae Afif,Jaber Lyahyai,Ilham Ratbi,Imane Cherkaoui Jaouad,Yassamine Doubaj,Meryem Sahli,Mouna Ouhenach,Abdelaziz sefiani

Breast Cancer Research and Treatment（2022）

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